The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

Ferricyanide     iron(+3) cation hexacyanide

Synonyms: CHEBI:5020, CPD-10145, C00324, [Fe(CN)6](3-), 13408-62-3, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of Ferric hexacyanide

  • Elevated concentrations of Proteus vulgaris, either as free cells or immobilised in Lentikat disks, were incubated with an excess of redox mediator (potassium hexacyanoferrate(III)) and organic substrate for 1h at 37 degrees C without oxygen [1].
  • Elevated concentrations of Escherichia coli were incubated with an excess of redox mediator, potassium hexacyanoferrate(III), and a known substrate for 1 h at 37 degrees C without oxygen [2].
 

High impact information on Ferric hexacyanide

 

Biological context of Ferric hexacyanide

 

Associations of Ferric hexacyanide with other chemical compounds

 

Analytical, diagnostic and therapeutic context of Ferric hexacyanide

References

  1. MICREDOX--development of a ferricyanide-mediated rapid biochemical oxygen demand method using an immobilised Proteus vulgaris biocomponent. Pasco, N., Baronian, K., Jeffries, C., Webber, J., Hay, J. Biosensors & bioelectronics. (2004) [Pubmed]
  2. Biochemical mediator demand--a novel rapid alternative for measuring biochemical oxygen demand. Pasco, N., Baronian, K., Jeffries, C., Hay, J. Appl. Microbiol. Biotechnol. (2000) [Pubmed]
  3. The B form of dihydroorotate dehydrogenase from Lactococcus lactis consists of two different subunits, encoded by the pyrDb and pyrK genes, and contains FMN, FAD, and [FeS] redox centers. Nielsen, F.S., Andersen, P.S., Jensen, K.F. J. Biol. Chem. (1996) [Pubmed]
  4. The study of 1-electron equivalent oxidation-reduction reactions by fast pulse generation of reagents. Cytochrome c/ferri-ferrocyanide system. Ilan, Y., Shafferman, A., Stein, G. J. Biol. Chem. (1976) [Pubmed]
  5. A sensitive staining method for NORs. Yekeler, H., Erel, O., Yumbul, A.Z., Doymaz, M.Z., Doğan, O., Ozercan, M.R., Iplikçi, A. J. Pathol. (1995) [Pubmed]
  6. Versatile apoferritin nanoparticle labels for assay of protein. Liu, G., Wang, J., Wu, H., Lin, Y. Anal. Chem. (2006) [Pubmed]
  7. Effect of pre-treatment on the surface and electrochemical properties of screen-printed carbon paste electrodes. Cui, G., Yoo, J.H., Lee, J.S., Yoo, J., Uhm, J.H., Cha, G.S., Nam, H. The Analyst. (2001) [Pubmed]
  8. Automated kinetic-spectrofluorimetric method for the determination of morphine in urine. Cepas, J., Silva, M., Pérez-Bendito, D. The Analyst. (1993) [Pubmed]
  9. Studies on the preparation of bioactive lignans by oxidative coupling reaction. IV. Oxidative coupling reaction of methyl (E)-3-(3,4-dihydroxy-2-methoxyphenyl)propenoate and lipid peroxidation inhibitory effects of the produced lignans. Maeda, S., Masuda, H., Tokoroyama, T. Chem. Pharm. Bull. (1995) [Pubmed]
  10. Elution and decomposition of cyanide in soil contaminated with various cyanocompounds. Matsumura, M., Kojima, T. Journal of hazardous materials. (2003) [Pubmed]
  11. 4-(6,7-Dihydro-5,8-dioxothiazolo[4,5-g]phthalazin-2-yl)benzoic acid N-hydroxysuccinimide ester as a highly sensitive chemiluminescence derivatization reagent for amines in liquid chromatography. Yoshida, H., Nakao, R., Matsuo, T., Nohta, H., Yamaguchi, M. Journal of chromatography. A. (2001) [Pubmed]
  12. Production of glycolate by oxidation of the 1,2-dihydroxyethyl-thamin-diphosphate intermediate of transketolase with hexacyanoferrate(III) or H2O2. Christen, P., Gasser, A. Eur. J. Biochem. (1980) [Pubmed]
  13. Determination of norepinephrine in microdialysis samples by microbore column liquid chromatography with fluorescence detection following derivatization with benzylamine. Yamaguchi, M., Yoshitake, T., Fujino, K., Kawano, K., Kehr, J., Ishida, J. Anal. Biochem. (1999) [Pubmed]
  14. Type III Cu mutants of Myrothecium verrucaria bilirubin oxidase. Shimizu, A., Samejima, T., Hirota, S., Yamaguchi, S., Sakurai, N., Sakurai, T. J. Biochem. (2003) [Pubmed]
  15. Determination of vitamin B6 in pharmaceutical formulations by flow injection-solid phase spectrophotometry. Portela, J.G., Costa, A.C., Teixeira, L.S. Journal of pharmaceutical and biomedical analysis. (2004) [Pubmed]
  16. Synergistic substrates determination with biosensors. Kulys, J., Tetianec, L. Biosensors & bioelectronics. (2005) [Pubmed]
  17. Determination of polyphenols by high-performance liquid chromatography with inhibited chemiluminescence detection. Cui, H., He, C., Zhao, G. Journal of chromatography. A. (1999) [Pubmed]
  18. Fluorescence analysis of p-hydroxymethamphetamine in urine by thin-layer chromatography. Kato, N., Kubo, H., Homma, H. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry. (2005) [Pubmed]
 
WikiGenes - Universities